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About This Item
Empirical Formula (Hill Notation):
C6H4F3NO
CAS Number:
Molecular Weight:
163.10
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
solid
mp
48-50 °C (lit.)
SMILES string
FC(F)(F)C(=O)c1ccc[nH]1
InChI
1S/C6H4F3NO/c7-6(8,9)5(11)4-2-1-3-10-4/h1-3,10H
InChI key
UMVVPYXSJKIFST-UHFFFAOYSA-N
Related Categories
General description
2-(Trifluoroacetyl)pyrrole, an α,α,α-trifluoromethyl ketone is a 2-substituted pyrrole derivative. It has been synthesized by reacting pyrrole with trifluoroacetic anhydride in benzene at 0°C. Its enantioselective hydrogenation to form corresponding alcohol using 5wt.% Pt/Al2O3 catalyst chirally modified by new synthetic chiral amines has been investigated.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Find documentation for the products that you have recently purchased in the Document Library.
Preparation of Indazoles and Quinazolines by Catalytic Dehydrogenation.
Burnett JrJ and Ainsworth C.
The Journal of Organic Chemistry, 23(9), 1382-1383 (1958)
Chemo and enantioselective hydrogenation of fluorinated ketones on platinum modified with (R)-1-(1-naphthyl) ethylamine derivatives.
Diezi S, et al.
J. Mol. Catal. A: Chem., 239(1), 49-56 (2005)
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